ClinVar Miner

List of variants reported as uncertain significance for Epilepsy, childhood absence, susceptibility to, 5

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_021912.5(GABRB3):c.31C>T (p.Pro11Ser)	rs25409	0.00354
NM_000814.6(GABRB3):c.486G>C (p.Met162Ile)	rs2140737836
NM_000814.6(GABRB3):c.880C>T (p.Arg294Trp)

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